3-Chlorothiophene-2-carbonyl chloride → 5-[5-(3-Chloro-2-thienyl)-1,2,4-oxadiazol-3-yl]-2-methoxypyridine
Reaction equation
[Cl:1][C:2]1[CH:6]=[CH:5][S:4][C:3]=1[C:7](Cl)=[O:8].[CH3:10][O:11][C:12]1[N:17]=[CH:16][C:15]([C:18](=[N:20]O)[NH2:19])=[CH:14][CH:13]=1>>[Cl:1][C:2]1[CH:6]=[CH:5][S:4][C:3]=1[C:7]1[O:8][N:19]=[C:18]([C:15]2[CH:16]=[N:17][C:12]([O:11][CH3:10])=[CH:13][CH:14]=2)[N:20]=1Participants
3
Procedure
The title compound was prepared as in Example 16 from 3-chloro-thiophene-2-carbonyl chloride (0.150 g, 0.828 mmol) and 6-methoxy-pyridine-3-amidoxime (0.138 g, 0.828 mmol) as a white solid (166 mg, 63%).
Sources & evidence
- ORD record
- ord-96b91005dbf741d6ba50723b6f148428
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435750B2
Reaction notes
Loading…